Assessing Phenotypic and Genotypic Resistance to Flumethrin in <i>Varroa destructor</i> Populations in Muğla, Türkiye

Beekeepers use a variety of methods to control <i>Varroa destructor</i> (varroa). Chemical control relies heavily on flumethrin, amitraz, coumaphos, and tau-fluvalinate products. However, increasing colony losses in recent years have been linked to the development of resistance in varroa...

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Main Authors: Ali Sorucu, Bekir Çöl, Esra Dibek, Anara Babayeva
Format: Article
Language:English
Published: MDPI AG 2025-05-01
Series:Insects
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Online Access:https://www.mdpi.com/2075-4450/16/6/548
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author Ali Sorucu
Bekir Çöl
Esra Dibek
Anara Babayeva
author_facet Ali Sorucu
Bekir Çöl
Esra Dibek
Anara Babayeva
author_sort Ali Sorucu
collection DOAJ
description Beekeepers use a variety of methods to control <i>Varroa destructor</i> (varroa). Chemical control relies heavily on flumethrin, amitraz, coumaphos, and tau-fluvalinate products. However, increasing colony losses in recent years have been linked to the development of resistance in varroa mites to these insecticides. Varroa mites develop mutations in the voltage-gated sodium channel (VGSC) that confer resistance to pyrethroids such as flumethrin. Specifically, researchers have identified substitutions of the leucine amino acid at VGSC L925 with isoleucine, methionine, or valine. This study investigated phenotypic and genotypic resistance to flumethrin in varroa populations in Muğla, Türkiye. LD<sub>50</sub> values (lethal dose for 50% mortality) were quantified, and PCR and sequencing were used to analyze the VGSC L925 gene region. The PCR results confirmed mutations in the target gene region in all samples. Sequencing revealed that 95% of the population carried homozygous resistant alleles, while 5% were heterozygous. At the VGSC L925 locus, leucine was replaced by isoleucine (91%), methionine (6%), and valine (3%). Phenotypic assays showed an average LD<sub>50</sub> value of 49.1 µg (range: 31–61.8 µg). Comparison of LD<sub>50</sub> between resistant and susceptible populations was not possible because no susceptible individuals were identified. Despite the resistance, mortality increased with escalating doses, suggesting that current protocols may be temporarily mitigating infestations. However, urgent dose adjustments and alternative control strategies are critical to prevent imminent colony collapse.
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spelling doaj-art-62b35cd51de04b529f6bc5a5dc1bcce42025-08-20T03:27:33ZengMDPI AGInsects2075-44502025-05-0116654810.3390/insects16060548Assessing Phenotypic and Genotypic Resistance to Flumethrin in <i>Varroa destructor</i> Populations in Muğla, TürkiyeAli Sorucu0Bekir Çöl1Esra Dibek2Anara Babayeva3Department of Pharmacology and Toxicology, Faculty of Milas Veterinary Medicine, Muğla Sitki Koçman University, Muğla 48200, TürkiyeDepartment of Biology, Faculty of Science, Muğla Sitki Koçman University, Muğla 48100, TürkiyeBiotechnology Research Centre, Muğla Sitki Koçman University, Muğla 48100, TürkiyeBiotechnology Research Centre, Muğla Sitki Koçman University, Muğla 48100, TürkiyeBeekeepers use a variety of methods to control <i>Varroa destructor</i> (varroa). Chemical control relies heavily on flumethrin, amitraz, coumaphos, and tau-fluvalinate products. However, increasing colony losses in recent years have been linked to the development of resistance in varroa mites to these insecticides. Varroa mites develop mutations in the voltage-gated sodium channel (VGSC) that confer resistance to pyrethroids such as flumethrin. Specifically, researchers have identified substitutions of the leucine amino acid at VGSC L925 with isoleucine, methionine, or valine. This study investigated phenotypic and genotypic resistance to flumethrin in varroa populations in Muğla, Türkiye. LD<sub>50</sub> values (lethal dose for 50% mortality) were quantified, and PCR and sequencing were used to analyze the VGSC L925 gene region. The PCR results confirmed mutations in the target gene region in all samples. Sequencing revealed that 95% of the population carried homozygous resistant alleles, while 5% were heterozygous. At the VGSC L925 locus, leucine was replaced by isoleucine (91%), methionine (6%), and valine (3%). Phenotypic assays showed an average LD<sub>50</sub> value of 49.1 µg (range: 31–61.8 µg). Comparison of LD<sub>50</sub> between resistant and susceptible populations was not possible because no susceptible individuals were identified. Despite the resistance, mortality increased with escalating doses, suggesting that current protocols may be temporarily mitigating infestations. However, urgent dose adjustments and alternative control strategies are critical to prevent imminent colony collapse.https://www.mdpi.com/2075-4450/16/6/548<i>Varroa destructor</i>resistanceflumethrinphenotypicgenotypic
spellingShingle Ali Sorucu
Bekir Çöl
Esra Dibek
Anara Babayeva
Assessing Phenotypic and Genotypic Resistance to Flumethrin in <i>Varroa destructor</i> Populations in Muğla, Türkiye
Insects
<i>Varroa destructor</i>
resistance
flumethrin
phenotypic
genotypic
title Assessing Phenotypic and Genotypic Resistance to Flumethrin in <i>Varroa destructor</i> Populations in Muğla, Türkiye
title_full Assessing Phenotypic and Genotypic Resistance to Flumethrin in <i>Varroa destructor</i> Populations in Muğla, Türkiye
title_fullStr Assessing Phenotypic and Genotypic Resistance to Flumethrin in <i>Varroa destructor</i> Populations in Muğla, Türkiye
title_full_unstemmed Assessing Phenotypic and Genotypic Resistance to Flumethrin in <i>Varroa destructor</i> Populations in Muğla, Türkiye
title_short Assessing Phenotypic and Genotypic Resistance to Flumethrin in <i>Varroa destructor</i> Populations in Muğla, Türkiye
title_sort assessing phenotypic and genotypic resistance to flumethrin in i varroa destructor i populations in mugla turkiye
topic <i>Varroa destructor</i>
resistance
flumethrin
phenotypic
genotypic
url https://www.mdpi.com/2075-4450/16/6/548
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